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Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders
Recently discovered genome-wide rare copy number variants (CNVs) have unprecedented levels of statistical association with many developmental neuropsychiatric disorders, including schizophrenia, autism spectrum disorders, intellectual disability and attention deficit hyperactivity disorder. However,...
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| Main Authors: | , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2013
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3852900/ https://ncbi.nlm.nih.gov/pubmed/23917946 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/mp.2013.92 |
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